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nsv5425133

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:93

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 124 SVs from 27 studies. See in: genome view    
Submitted genomic46,270,708-46,270,800Question Mark
Overlapping variant regions from other studies: 124 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):46,736,380-46,736,472Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5425133Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr146,270,70846,270,800
nsv5425133RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr146,736,38046,736,472

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16901847duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16901847Submitted genomicNC_000001.11:g.462
70708_46270800dup
GRCh38 (hg38)NC_000001.11Chr146,270,70846,270,800
nssv16901847RemappedPerfectNC_000001.10:g.467
36380_46736472dup
GRCh37.p13First PassNC_000001.10Chr146,736,38046,736,472

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv169018470.005356404
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